DISTROFIA MUSCULAR DE STEINERT PDF

La distrofia muscular es un trastorno genético que debilita de forma como enfermedad de Steinert: se trata del tipo distrofia muscular más frecuente en la.

Author: Kagazragore Vizahn
Country: Philippines
Language: English (Spanish)
Genre: Health and Food
Published (Last): 25 September 2018
Pages: 325
PDF File Size: 8.71 Mb
ePub File Size: 18.52 Mb
ISBN: 594-4-91510-490-8
Downloads: 19348
Price: Free* [*Free Regsitration Required]
Uploader: Terisar

Curr Opin Neurol, 10pp. A study of ten cases.

Disstrofia hydramnios in association with myotonia dystrophica. J Reprod Med, 28pp. Neonatal myotonic dystrophy as a cause of hydramnios and neonatal death. Are you a health professional able to prescribe or dispense drugs?

J Gynecol Obstet Biol Reprod, 24pp. The congenital form has a poor prognosis, and is more difficult to diagnose. Am J Obstet Gynecol, 82pp.

Distrofia muscular

J Pediatr Ophthalmol Strabismus, 31pp. Congenital myotonic dystrophy in Britain. Molecular basis of miotonic dystrophy: The movements of fetuses with congenital myotonic dystrophy in utero. Diagnostic problems in congenital myotonic dystrophy.

Five cases in preterm babies and review of early reports. Arch Dis Child, 54 dustrofia, pp.

  CVISION COMPRESS PDF

Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy. Dystrophia myotonica and pregnancy [abstract]. Three times of anesthetic management in a patient with myotonic dystrophy [abstract].

Distrofua, 84pp. First-trimester prediction in fetus at risk for myotonic dystrophy. Arch Dis Child, 67pp. Cell, 68pp.

Distrofia miotónica de steinert y gestación | Clínica e Investigación en Ginecología y Obstetricia

Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. Complex relationships between clinical findings and structure of the Steibert repeat. Van de Biezenbos, J. Prenat Diagn, 13pp. Signs of fetal affectation during pregnancy are hydrops, hydramnios, a reduction in fetal movements, and a slow fetal heart rate. Ann Neurol, 35pp.

Distrofia muscular (para Padres)

To improve our services and products, we use ristrofia own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. Masui, 51pp. A case report and recent literature.

Principios de medicina interna, pp. Obstet Gynecol, 45pp. Pediatr Neurol, 12pp. Lancet, 2pp. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. Eguiluz aW. Prenatal diagnosis of myotonic dystrophy by direct mutation analysis.

  LEYES DE LA SIMPLICIDAD MAEDA PDF

Prenat Diagn, 11pp. Clinical expression of myotonic dystrophy: Clin Invest Ginecol Obstet, 25pp. Lancet, 1 muschlar, pp. Minerva Pediatr, 53pp. Si continua navegando, consideramos que acepta su uso.

Ultras Obstet Gyneacol [en prensa]. Obstetric musular as the first sign of myotonic dystrophy. Am J Obstet Gynecol,pp. Acta Obstet Gynecol Scand, 65pp. Myotonic dystrophy is a significant cause of idiopatic polyhydramnios.

Semin Pediatr Setinert, 3pp. Anticipation in myotonic dystrophy. Lancet,pp. Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion.